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KUMMAS Bipolar Forceps - Indonesia BPOM Medical Device Registration

KUMMAS Bipolar Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603916705. The device is manufactured by KUMMAS CORPORATION from Pakistan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SOMETECH NEW Zealand.

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BPOM Registered
Risk Class Kelas Resiko : C
KUMMAS Bipolar Forceps
Analysis ID: AKL 21603916705

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

KUMMAS CORPORATION

Country of Origin

Pakistan

Authorized Representative

SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530

Registration Date

Jun 21, 2024

Expiry Date

Apr 16, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Electromedic Non Sterile

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